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Dapagliflozin ((2S)-1,2-propanediol, hydrate)

    
99.90%

Dapagliflozin ((2S)-1,2-propanediol, hydrate)

源叶(MedMol)
S81172 一键复制产品信息
960404-48-2
C24H35ClO9
502.9823
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S81172-5mg买3赠1
99.90%

¥350.00

>10 - - - -
S81172-10mg买3赠1
99.90%

¥500.00

>10 - - - -
S81172-50mg买3赠1
99.90%

¥1290.00

>10 - - - -
S81172-250mg买3赠1
99.90%

¥3200.00

>10 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: Dapagliflozin propanediol belongs to the class of orally administered antidiabetic agents designated as sodiumglucose cotransporter 2 (SGLT2) inhibitors
靶点: SGLT2;SGLT
体外研究: Dapagliflozin is a small-molecule inhibitor of SGLT2 that has been shown to be highly selective for SGLT2 compared with other SGLT family members and to have no off-target interactions in an in vitro screen of more than 330 receptors, enzymes, ion channels, and transporters
体内研究: Dapagliflozin demonstrates good oral bioavailability, has a high volume of distribution, and has an in vivo metabolite profile that is qualitatively similar between preclinical species and humans. Both non-clinical and clinical assessments have shown dapagliflozin to have a highly favorable safety profile that is consistent with its simple mechanism of action, with no off-target effects observed
动物实验: Animal Models: Sprague-Dawley (SD) rats Dosages: 25, 100, 150, or 200 mg/kg Administration: oral
参考文献: 1. Reilly TP, et al. Carcinogenicity risk assessment supports the chronic safety of dapagliflozin, an inhibitor of sodium-glucose co-transporter 2, in the treatment of type 2 diabetes mellitus. Diabetes Ther. 2014, 5(1):73-96.
溶解性: Soluble  in  DMSO、Ethanol
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.988 ml 9.941 ml 19.881 ml
5 mM 0.398 ml 1.988 ml 3.976 ml
10 mM 0.199 ml 0.994 ml 1.988 ml
50 mM 0.04 ml 0.199 ml 0.398 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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